rs3864663

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs3864663(C;C)

Make rs3864663(C;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

77768114

is a	snp
is	mentioned by
dbSNP	rs3864663
dbSNP (classic)	rs3864663
ClinGen	rs3864663
ebi	rs3864663
HLI	rs3864663
Exac	rs3864663
Gnomad	rs3864663
Varsome	rs3864663
LitVar	rs3864663
Map	rs3864663
PheGenI	rs3864663
Biobank	rs3864663
1000 genomes	rs3864663
hgdp	rs3864663
ensembl	rs3864663
geneview	rs3864663
scholar	rs3864663
google	rs3864663
pharmgkb	rs3864663
gwascentral	rs3864663
openSNP	rs3864663
23andMe	rs3864663
SNPshot	rs3864663
SNPdbe	rs3864663
MSV3d	rs3864663
GWAS Ctlg	rs3864663

GMAF

0.05464

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21658281]
Trait
Title	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Risk Allele
P-val	0.000002
Odds Ratio	1.4000 [1.22-1.61]